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J. Biol. Chem., Vol. 278, Issue 28, 26065-26070, July 11, 2003
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From the Departamento de Genética y Biología Molecular, Centro de Investigación y de Estudios Avanzados del IPN, Apartado Postal 14–740, México Distrito Federal 07000
Received for publication, February 3, 2003 , and in revised form, April 16, 2003.
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONEXPERIMENTAL PROCEDURESRESULTSDISCUSSIONREFERENCES |
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONEXPERIMENTAL PROCEDURESRESULTSDISCUSSIONREFERENCES |
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Translation of two-codon minigenes located in bacteriophage lambda chromosome bar regions is lethal to cells partly defective in peptidyl-tRNA hydrolase activity, but not to wild-type bacteria (3). Translation of bar minigene mRNAs results in premature release of peptidyl-tRNAs from ribosomes (a phenomenon called "drop-off"); under limited Pth1 activity, these peptidyl-tRNAs accumulate in the cell. It has been proposed that lethality stems from the subsequent shortage in the pool of specific tRNAs for further involvement in protein synthesis (4). Recently, evidence that seems to support this inference has been obtained for a ribosome bypassing system (5), but the alternative explanation that peptidyl-tRNAs might be toxic per se has not been ruled out (6).
Translation ends at the termination codon in an mRNA, when the ribosomal peptidyl-transferase presumably hydrolyzes the ester bond between the completed polypeptide chain and the last tRNA. The termination reaction requires the concurrence of the release factors RF-1 or RF-2 (depending on the nature of the termination codon) and other factors catalyzing the release of the mature protein (7, 8). Drop-off is a normal, if relatively rare, event in protein synthesis that can occur during elongation or instead of polypeptide termination (9, 10). If the rates of peptidyl-tRNA synthesis and drop-off exceed the rates of termination and Pth hydrolysis, peptidyl-tRNA accumulates and thus critically reduces the concentration of aminoacylable tRNA and increases that of peptidyl-tRNAs (4, 9). The up-shift to non-permissive temperatures of a thermosensitive pth mutant, pth(Ts), results in peptidyl-tRNA buildup of all the tRNAs assayed. The rates of peptidyl-tRNA accumulation differ as a function of the tRNA species. Thus, families of tRNA cognate to codons for Lys, Thr, and Asn accumulate the fastest, whereas those cognate to codons for Leu, Gly, and Cys accumulate the slowest (11). These results suggest that the drop-off rates depend on the codons involved.
Toxicity and peptidyl-tRNA accumulation in the pth(Ts) mutant is alleviated in strains defective for the translation termination factors RF-3 and RRF (12). Drop-off during minigene mRNA translation is enhanced by these termination factors as well as the elongation factor EF-G (9). In vitro experiments with different synthetic minigenes have shown that the relative rates of termination and drop-off vary according to the composition of the last sense codon, the nature and context of the stop codon, and the length of the mini-ORF and that toxicity is correlated to these conditions (9, 13). In addition, the strong effect of the SD sequence affects peptidyl-tRNA accumulation by driving minigene mRNA through several rounds of translation without dissociation from the ribosome (9). Despite these results, the scarce number and heterogeneity of minigenes studied so far does not allow us to draw conclusions about the role of codon composition in drop-off. We have studied the effect of the last sense codon on peptidyl-tRNA accumulation, minigene mRNA concentration, translation termination, and toxicity to pth-defective cells. Our results indicate that the degree of toxicity stems from the intrinsic inability of certain codon-tRNA complexes to mediate efficient translation termination.
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EXPERIMENTAL PROCEDURES |
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TOPABSTRACTINTRODUCTIONEXPERIMENTAL PROCEDURESRESULTSDISCUSSIONREFERENCES |
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Minigene Library Construction—The complete set of 64 constructs harboring two-codon minigenes was obtained by cloning duplex synthetic oligos into vector pKQV4, which carries the IPTG-inducible tac promoter (Fig. 1A; Ref. 17). An attempt was made to generate the 64 pairs of complementary synthetic oligos, namely 5'-AATTCATGNNNTAAATA-3' and 5'-AGCTTATTTANNNCATG-3' (the EcoRI and HindIII cohesive ends are underlined and in bold, respectively), by random synthesis at positions NNN corresponding to the variable minigene codon (Fig. 1A). Duplexes were obtained by allowing complementary oligos to hybridize in a mixture containing 400 pmol of each random oligo in 100 µl of buffer (10 mM Tris-HCl, pH 7.2, 1 mM EDTA) for 5 min at 95 °C and slowly cooled down to room temperature. Duplexes were then cloned into the vector after their double restriction digestion with both EcoRI and HindIII. Ligation of inserts into this vector was performed using 40 fmol of duplex mixture with 15 fmol of the double-restricted vector in 20 µl of buffer (10 mM Tris-HCl, pH 7.2, 1 mM ATP, 10 mM magnesium acetate, 25 mM NaCl, and 10 units of T4 DNA ligase (Amersham Biosciences)) for 1 h at room temperature. The ligation mix was used to transform C6OOrap cells (18), and selected clones were tested for the absence of the SalI site present in the unsubstituted vector only. Inserts from these clones were sequenced using Big-Dye sequencing kits (Applied Biosystems), using the forward oligo 5'-GACATAACGGTTCTGGC-3', corresponding to a sequence close to Ptac, and the reverse oligo 5'-CTGTTTTATCAGACCGC-3', corresponding to a sequence upstream to the 5 S gene (Fig. 1A). Thirty-two minigenes were obtained after random hybridization, and the rest were obtained by direct cloning of specific duplexes into the expression vector as described above.
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Peptidyl-tRNA Levels—Peptidyl-tRNA levels were estimated by a modification of the Northern blot technique of Varshney et al. (19). This method is more specific than the traditional assay (20), because it distinguishes individual tRNAs. Briefly, the transformants for minigene constructs were cultured on LB (100 µg/ml ampicillin) at 32 °C to an A600 value of 0.5 and induced with 1 mM IPTG for different periods of time (see "Results") at 32 °C. To estimate the fraction of peptidyl-tRNA relative to total tRNA, aminoacyl-tRNAs were hydrolyzed by the cupric reaction (21). Total extracted tRNA was resuspended in 20 µl of water and divided into two aliquots: a control sample that was mixed with 90 µl of 20 mM sodium acetate, pH 5.0, and a hydrolysis sample with 10 mM CuSO4. Each reaction was incubated for 30 min at 37 °C and was precipitated with 2 volumes of ethanol after addition of EDTA to a final concentration of 5 mM. The samples were resolved by acid/urea PAGE and transferred to nylon membranes; tRNA-containing species were revealed using specific 32P-labeled oligo probes (5 x 106 cpm/pmol; Refs. 19 and 22). The peptidyl-tRNA fraction was estimated from the radioactivity ratio between the measured radioactivities in the (peptidyl-tRNA/peptidyl-tRNA + tRNA) respective bands as determined in a Typhoon Scan (Amersham Biosciences).
Minigene mRNA Detection—Total RNA was obtained from cultures
of transformants for minigene constructs induced with IPTG. Minigene mRNA was
revealed by Northern blot analysis using a 32P-labeled DNA probe (2
x 106 cpm/ng; Ref.
23). The 150-bp DNA probe was
synthesized by 50 cycles of PCR (95 °C, 30 s; 55 °C, 30 s and 72
°C, 1 min) using 30 fmol of pKQV4 template and 10 pmol of each sequencing
oligo (defined above) in a 50-µl reaction mixture containing 40
mM Tris-HCl, pH 8.0, 5 mM MgCl2, 10
mM dithiothreitol, 50 mM NaCl, 50 µCi of
[
-32P]dCTP (6,000 Ci/mmol, Amersham Biosciences), 150
µM concentration each of the other three dNTPs, and 1 unit of
Taq DNA polymerase (Applied Biosystems).
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RESULTS |
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TOPABSTRACTINTRODUCTIONEXPERIMENTAL PROCEDURESRESULTSDISCUSSIONREFERENCES |
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Non-toxic Minigenes Do Not Mediate Peptidyl-tRNA Accumulation—For a number of minigenes, a direct correlation between toxicity and peptidyl-tRNA concentration has been observed in pth mutants (4, 9, 24). To assess the breadth of this observation, we estimated the relative concentrations of peptidyl-tRNAs for selected minigenes. Initially, we determined the time length of IPTG minigene induction which generated the highest peptidyl-tRNA concentrations. The data showed that, for the toxic (AAT and AAA) and partly toxic (GAT and GAA) minigenes assayed, the highest accumulated fraction was reached in all cases within a 30-min induction period (Fig. 2B). Therefore, all subsequent determinations of peptidyl-tRNA concentration were made at 30 min (Fig. 1B, columns 4 and 5). The relative concentrations of peptidyl-tRNA in C600pth(Ts) varied from 40 to 70% for toxic, 10 to 20% for partly toxic, and 5 and 10% for non-toxic minigenes (Fig. 1B, fourth column in each cell). In C600rap, the relative concentrations of peptidyl-tRNA from toxic and partly toxic minigenes were proportionally higher (Fig. 1B, fifth column in each cell), whereas the concentrations of peptidyl-tRNA for non-toxic minigenes were lower, although similar to those observed for pth(Ts). Wild-type transformants did not accumulate peptidyl-tRNA (data not shown). Except for minigene AAT, encoding Asn, which intriguingly promotes accumulation of peptidyl-tRNALys (Fig. 2A), heterologous peptidyl-tRNAs did not accumulate upon minigene expression: minigene AAA did not accumulate peptidyl-tRNAAsn; minigene GAT did not accumulate peptidyl-tRNAGlu; minigene GAA did not mediate accumulation of peptidyl-tRNAAsp (Fig. 2A); and minigene AGA did not accumulate peptidyl-tRNALys.
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Peptidyl-tRNA Accumulation Depends upon the Specific Codon-tRNA Interaction—In six of the genetic code boxes (dashed boxes in Fig. 1B), minigenes showed mixed degrees of toxicity. To understand the basis of these differences, we analyzed peptidyl-tRNA accumulation upon minigene induction in Pth-defective mutants. For example, in the set of minigenes carrying Arg codons CGU, CGC, and CGA, for which tRNAArg-2 is the sole cognate species, the generated peptidyl-tRNAs must be chemically identical. If we assume an equal decoding rate for the mini-ORFs in each of the three minigenes, toxicity would depend on the drop-off rate, because the rate of peptidyl-tRNA hydrolysis by Pth is identical. The relative amounts of peptidyl-tRNAArg-2 accumulated after expression of each minigene in Pth-defective strains ranked in the order CGA>CGT>CGC, as expected from their degree of toxicity (Fig. 3). Accordingly, the peptidyl-tRNA concentrations should reflect the rate of peptidyl-tRNAArg-2 drop-off due to differences in tRNAArg-2 interaction with each of the three codons (see "Discussion").
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tRNASer-1 is cognate to the codons in partly toxic minigenes TCT and TCA and clearly accumulates as peptidyl-tRNASer-1 in strain pth(rap) (40%, Fig. 1B); by contrast, accumulation of peptidyl-tRNASer-5, produced by both the partly toxic TCT and the non-toxic TCC minigenes, was not promoted in either strain (Fig. 1B). This suggests strongly that the toxicity of minigenes TCT and TCA is associated with peptidyl-tRNASer-1 accumulation. The data for the minigenes CTA and CTG could be explained in a similar way.
Non-toxic Minigene mRNAs Are Translated—For the expression of different minigene variants, the cellular levels and stability of minigene mRNA correlate with the strength of toxicity. It has been speculated that the increased messenger stability results from a longer interaction period with the ribosome during translation (25). Results with Northern blot assays confirmed that toxic minigenes (e.g. AAA, GTT, and CGA) accumulated high levels of mRNA, whereas non-toxic minigenes (e.g. GCC, GGC, and CGC) did not (data not shown). We then asked whether non-toxic minigene mRNAs were translated at all and, if they were, why their expression did not drive peptidyl-tRNA accumulation. Minigene AGA, lethal to C600pth(Ts), and the non-lethal minigene GGC, were expressed in the presence of antibiotics (Fig. 4). The antibiotics used were pactamycin, which causes ribosome stalling soon after initiation of protein synthesis (27), and erythromycin, which enhances the dissociation of peptidyl-tRNAs containing at least six to eight amino acids (6, 28). As expected, the expression of the lethal minigene AGA resulted in mRNA accumulation even in the absence of the antibiotics. The non-toxic GGC minigene, on the other hand, accumulated mRNA only in the presence of pactamycin. Similar results were obtained with the lethal CGA and the non-toxic CGC minigenes (data not shown). These results indicate that mRNAs of these non-toxic minigenes are translatable; furthermore, in the absence of antibiotics translation termination should have occurred readily, suggesting that the mRNA-ribosome complex may be short lived. Erythromycin did not mediate accumulation of peptidyl-tRNA nor did it stabilize the ribosome-mRNA complex as deduced from the observation that it did not favor mRNA accumulation (Fig. 4). Given that the erythromycin binding site is at the entrance of the 50 S ribosomal subunit tunnel (29), it is not expected to affect dipeptidyl-tRNAs which are too short to reach the site.
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Efficient Translation Termination Prevents Peptidyl-tRNA Accumulation—To test whether toxic and non-toxic minigenes differ in the efficiency of translation termination, the levels of peptidyl-tRNA, the intermediate previous to termination hydrolysis, were assayed under a condition of defective termination (Fig. 5). An E. coli prfA1-pth(rap) double mutant, defective for both RF1 (thermosensible) and Pth activities, was transformed with constructs carrying minigenes causing different degrees of lethality. In mutant prfA1 the activity of RF1 is greatly reduced at 43 °C (16). We used the partly toxic CGT minigene and the non-toxic variant CGC, for which tRNAArg-2 is the sole cognate isoacceptor. When RF1 was defective, expression at 32 °C of the CGC minigene did not promote detectable peptidyl-tRNAArg-2 accumulation, whereas it did at 43 °C (lane 4 versus lane 8). The partly toxic CGT minigene promoted peptidyl-tRNAArg-2 accumulation at both temperatures (lanes 2 and 6), and accumulation was enhanced at 43 °C. These results suggest that efficient translation termination of non-toxic minigene mRNAs shortens peptidyl-tRNA residence time on the ribosome so that drop-off events remain undetectable. In strain prfA1, which harbors the wild-type pth allele (lanes 10 and 12), no peptidyl-tRNA was identified during toxic minigene expression at 43 °C; this suggests that all the generated peptidyl-tRNA eventually dissociates from the ribosomes and is cleaved by Pth in solution.
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DISCUSSION |
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TOPABSTRACTINTRODUCTIONEXPERIMENTAL PROCEDURESRESULTSDISCUSSIONREFERENCES |
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A long ribosome pause on the last sense codon, arising from inefficient translation termination, eventually results in peptidyl-tRNA dissociation and mRNA stabilization (9, 12). Therefore, toxic minigenes would be defective in translation termination, and non-toxic minigenes would terminate readily. Additional support for this idea comes from two types of evidence: first, mRNA of the non-toxic CGC minigene was stabilized by pactamycin (data not shown), an antibiotic which arrests protein synthesis early after initiation and results in the accumulation of a 40 S·Met-tRNAF·mRNA complex (32); second, the expression of the same CGC minigene promoted the accumulation of normally undetectable peptidyl-tRNA under limited activity of the termination factor RF1 (Fig. 5, lanes 7 and 8; Ref. 16). We were unable to find a direct correlation between the minigene mRNA and peptidyl-tRNA accumulation, i.e. the length of the ribosomal pause and the strength of the codon:anticodon bond. If this strength has an influence on the ribosomal pause, it might be part of a more complex interaction which involves several factors. One factor could be the effect of both the amino acid side chains and the tRNA body of the peptidyl-tRNA on the interaction with the ribosome, in a manner similar to their themodynamic contribution to the binding of the aminoacyl-tRNA and the EF-Tu (33). A second factor affecting ribosomal pausing may be the specific architecture of the codon:anticodon interaction. The Arg codons CGA, CGU, and CGC are decoded by the unique tRNAArg-2 (22). Unlike CGC, CGA is a poor 5' context for amber suppression by the su7-encoded tRNA suggesting that the CGA codon-peptidyl-tRNAArg-2 in the ribosomal P-site can interfere with either the translation of a codon in the A site (34) or with enhanced termination at a stop codon. We showed that minigene CGA clearly promoted peptidyl-tRNA accumulation, whereas minigene CGC did not (Figs. 1B and 3), thus indicating that CGA hinders termination. It has been speculated that the A:I pairing of the CGA codon with the tRNAArg-2 anticodon at the wobble position is structurally distorted, thus hampering decoding (34, 35). Our results, however, showed that synthesis of peptidyl-tRNA occurs readily (Fig. 3), implying that the defect may be at mRNA translation termination. It is possible that wobble position base pair distortion affects translation termination, because minigene CGT, which accumulates intermediate levels of peptidyl-tRNA (Fig. 3), has a less severe distortion at the U:I pair in the CGU-anticodon interaction (34). A similar mechanism could apply for minigenes AGT and AGC, for which tRNASer-3 is the cognate species.
A third factor affecting ribosomal pausing could be the interaction between tRNA in the ribosomal P-site and the release factor in the A-site. For example, in the presence of peptidyl-tRNAGly-3 in the P-site at codons GGA/G, termination efficiency at UAG is higher than in the presence of peptidyl-tRNAGly-2 at the same codons, suggesting an unusual interaction between tRNAGly-2 and RF1 (36). This hypothesis could explain why toxicity and peptidyl-tRNA accumulation for TCT and CTG in the corresponding minigenes is associated to only one of the two cognate tRNAs (Fig. 1B).
What is the distribution of "toxic" and "non-toxic codons" in bacterial genes? Interestingly, AAA/G and AAU/AAC codons in minigenes, which promote high rates of peptidyl-tRNA accumulation (Fig. 2), are frequently located at the beginning of E. coli ORFs. These codons enhance efficiency of translation when substituted at positions two and three of a reporter gene (37, 38). By contrast, codons that promoted low rates of peptidyl-tRNA accumulation are rarely located among the first three positions (e.g. CUN, GCN, and GGN gene code boxes; Refs. 37 and 38). In the pth(ts) mutant, families of tRNAs cognate to these codons are among those with the lowest rates of accumulation of the corresponding peptidyl-tRNAs at non-permissive temperatures (11). The presence of codons prone to drop-off in minigenes may represent an advantage for protein synthesis when located at the initial positions in the mRNA ORFs. These codons might act as sensors of the general availability of charged tRNAs. If the availability is appropriate, elongation proceeds, otherwise abortive drop-off occurs. This strategy would prevent wasteful protein synthesis elongation under limiting tRNA availability.
Interestingly, a high frequency of AAA/G codons, associated to high drop-off rates in minigenes, has been found at the last sense position of the E. coli ORFs where they also promote drop-off (13). This non-random codon distribution at the ends of ORFs has been considered as an important factor in the modulation of translation termination (39). This could be explained, because such codons provide an alternative translation termination mechanism including drop-off and Pth-mediated hydrolysis of the final peptidyl-tRNA.
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FOOTNOTES |
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Supported by a postdoctoral fellowship from COSNET and funds from CONACyT
Grant O28.
During this time was a Université de Paris VII visiting professor and
was awarded a sabbatical fellowship by CONACyT. To whom correspondence should
be addressed. Tel.: 52-55-747-3338; Fax: 52-55-747-7100; E-mail:
guarnero{at}lambda.gene.cinvestav.mx.
1 The abbreviations used are: Pth, peptidyl-tRNA hydrolase; IPTG,
isopropyl-1-thio-
-D-galactopyranoside; ORF, open reading
frame; oligo, oligodeoxyribonucleotide; SD, Shine-Dalgarno sequence.
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ACKNOWLEDGMENTS |
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REFERENCES |
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TOPABSTRACTINTRODUCTIONEXPERIMENTAL PROCEDURESRESULTSDISCUSSIONREFERENCES |
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